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Synthesis and characterization of Co–Al–Fe nonstoichiometric spinel-type catalysts for catalytic CO oxidation

机译:Co-Al-Fe非晶体尖晶石型催化CO氧化催化剂的合成与表征

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A series of CoAlFe nonstoichiometric spinel-type oxides were synthesized from hydrotalcite precursors prepared through a co-precipitation method, and their catalytic activities for CO oxidation were investigated. The solids were characterized by XRD, BET, SEM, TG-DTG, H _(2) -TPR and in situ FTIR. The calcined hydrotalcite-like precursors were composed of spinel-like CoAlFe mixed oxide with crystallite sizes in the range 8–10.5 nm. The nanosized spinel oxide catalysts showed higher surface area as calcination led to dehydroxylation and carbonate decomposition of anions in interlayer spaces. FTIR results showed two vibrational frequency bands ( ν 1 and ν 2) for tetrahedral and octahedral sites, confirming the formation of the Co _(3) O _(4) spinel. Iron ions were introduced into the spinel system leading to improved redox properties, as confirmed by TPR. Furthermore, the CoAlFe ternary oxide nanoparticles exhibited superior catalytic performance in CO oxidation in contrast with CoAl and CoFe binary oxides, which can be ascribed to the improved reducibility. According to the in situ FT-IR analysis, CO adsorbed on the catalyst surface reacted with surface lattice oxygen to form CO _(2) . In addition, CO _(2) could adsorb on the surface and form intermediate carbonate species.
机译:通过通过共沉淀法制备的水滑石前体合成了一系列煤粉非煤矿型氧化物,研究了它们的共氧化催化活性。通过XRD,BET,SEM,TG-DTG,H _(2)-TPR和原位FTIR的特征在于固体。煅烧的水滑石样前体由尖晶石状煤灌注氧化物组成,其中微晶尺寸在8-10.5nm的范围内。纳米尖晶石氧化铝催化剂显示出较高的表面积,因为煅烧导致脱羟基化和层间空间中阴离子的碳酸盐分解。 FTIR结果表明,四面型和八面体位点显示了两种振动频带(ν1和ν2),确认了CO _(3)O _(4)尖晶石的形成。将铁离子引入尖晶石系统,导致氧化还原性能改善,如TPR所证实。此外,煤氟氢三元氧化物纳米颗粒在与煤和COFE二进制氧化物形成较好的催化性能,与煤和COFE二进制氧化物相比,这可以归因于改善的可还原性。根据原位FT-IR分析,CO吸附在催化剂表面上与表面晶格氧反应形成CO _(2)。另外,CO _(2)可以吸附在表面上并形成中间碳酸盐物种。

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